| NDC Code | 69842-963-01 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (69842-963-01) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE |
|---|
| Product NDC | 69842-963 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Mucus Dm Extended Release |
|---|
| Non-Proprietary Name | Guaifenesin, Dextromethorphan Hydrobromide |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190913 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207602 |
|---|
| Manufacturer | CVS Pharmacy |
|---|
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
|---|
| Strength | 30; 600 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
|---|